BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

309 related articles for article (PubMed ID: 11149132)

  • 21. Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome.
    Buzza M; Wilson D; Savige J
    Kidney Int; 2001 May; 59(5):1670-6. PubMed ID: 11318937
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial hematuric syndromes--Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes.
    Kashtan CE
    Contrib Nephrol; 2001; (136):79-99. PubMed ID: 11688406
    [No Abstract]   [Full Text] [Related]  

  • 23. [Collagen IV (alpha3-alpha4) nephropathy].
    Torra R; Tazón B; Ars E; Ballarín J
    Nefrologia; 2005; 25 Suppl 2():29-32. PubMed ID: 16050399
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.
    Gubler MC; Knebelmann B; Beziau A; Broyer M; Pirson Y; Haddoum F; Kleppel MM; Antignac C
    Kidney Int; 1995 Apr; 47(4):1142-7. PubMed ID: 7783412
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Variability of anti-GBM binding in hereditary nephritis.
    Jenis EH; Valeski JE; Calcagno PL
    Clin Nephrol; 1981 Mar; 15(3):111-4. PubMed ID: 7023765
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Immunohistologic findings in Alport syndrome.
    Kashtan CE; Kleppel MM; Gubler MC
    Contrib Nephrol; 1996; 117():142-53. PubMed ID: 8801043
    [No Abstract]   [Full Text] [Related]  

  • 27. Morphologic alterations and biochemical studies of the glomerular basement membrane in Alport syndrome.
    Spear GS
    Contrib Nephrol; 1990; 80():41-6. PubMed ID: 2282821
    [No Abstract]   [Full Text] [Related]  

  • 28. [Hereditary nephropathies].
    Yoshikawa N; Ito H; Nakamura N
    Pediatrie; 1990; 45(1):5-11. PubMed ID: 2158049
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular genetics of basement membranes: the paradigm of Alport syndrome.
    Antignac C
    Kidney Int Suppl; 1995 Jun; 49():S29-33. PubMed ID: 7674589
    [No Abstract]   [Full Text] [Related]  

  • 30. Evolution of glomerular basement membrane lesions in a male patient with Alport syndrome: ultrastructural and morphometric study.
    Cangiotti AM; Sessa A; Meroni M; Montironi R; Ragaiolo M; Mambelli V; Cinti S
    Nephrol Dial Transplant; 1996 Sep; 11(9):1829-34. PubMed ID: 8918631
    [No Abstract]   [Full Text] [Related]  

  • 31. Adenovirus-mediated transfer of type IV collagen alpha5 chain cDNA into swine kidney in vivo: deposition of the protein into the glomerular basement membrane.
    Heikkilä P; Tibell A; Morita T; Chen Y; Wu G; Sado Y; Ninomiya Y; Pettersson E; Tryggvason K
    Gene Ther; 2001 Jun; 8(11):882-90. PubMed ID: 11423936
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The thin glomerular basement membrane in children with haematuria.
    Yoshikawa N; Hashimoto H; Katayama Y; Yamada Y; Matsuo T; Okada S
    J Pathol; 1984 Apr; 142(4):253-7. PubMed ID: 6716210
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Absence of alpha 6(IV) collagen in kidney and skin of X-linked Alport syndrome patients.
    Hino S; Takemura T; Sado Y; Kagawa M; Oohashi T; Ninomiya Y; Yoshioka K
    Pediatr Nephrol; 1996 Dec; 10(6):742-4. PubMed ID: 8971895
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutations in type IV collagen genes and Alport phenotypes.
    Tryggvason K
    Contrib Nephrol; 1996; 117():154-71. PubMed ID: 8801044
    [No Abstract]   [Full Text] [Related]  

  • 35. Coexistence of thin membrane and alport nephropathies in families with haematuria.
    Moghal NE; Milford DV; White RH; Raafat F; Higgins R
    Pediatr Nephrol; 1999 Nov; 13(9):778-81. PubMed ID: 10603120
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis.
    Kalluri R; Shield CF; Todd P; Hudson BG; Neilson EG
    J Clin Invest; 1997 May; 99(10):2470-8. PubMed ID: 9153291
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.
    Kleppel MM; Kashtan CE; Butkowski RJ; Fish AJ; Michael AF
    J Clin Invest; 1987 Jul; 80(1):263-6. PubMed ID: 3298322
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hereditary nephritis mimicking immune complex-mediated glomerulonephritis.
    Nasr SH; Markowitz GS; Goldstein CS; Fildes RD; D'Agati VD
    Hum Pathol; 2006 May; 37(5):547-54. PubMed ID: 16647952
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A clinicopathological study of Alport syndrome and detection of type IV collagen chains in Alport patients.
    Chen N; Pan X; Ren H; Dong D
    Chin Med J (Engl); 1998 Sep; 111(9):797-802. PubMed ID: 11155669
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Immunohistochemical study of type IV collagen chain distribution within basement membrane in patients with Alport syndrome].
    Pan X; Chen N; Chen X
    Zhonghua Nei Ke Za Zhi; 1997 Dec; 36(12):812-5. PubMed ID: 10451936
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.